Crystallization behaviors of biodegradable poly(L-lactic acid)/graphene oxide nanocomposites from the amorphous state

被引:101
作者
Wang, Huishan [1 ]
Qiu, Zhaobin [1 ]
机构
[1] Beijing Univ Chem Technol, Minist Educ, State Key Lab Chem Resource Engn, Key Lab Carbon Fiber & Funct Polymers, Beijing 100029, Peoples R China
关键词
Biodegradable polymer; Crystallization; Graphene oxide; Nanocomposites; ENHANCED CRYSTALLIZATION; POLY(ETHYLENE SUCCINATE); HYDROLYTIC DEGRADATION; MELT CRYSTALLIZATION; COLD-CRYSTALLIZATION; CARBON NANOTUBES; ISOTHERMAL COLD; GRAPHENE; COMPOSITE;
D O I
10.1016/j.tca.2011.10.006
中图分类号
O414.1 [热力学];
学科分类号
摘要
Crystallization behaviors of biodegradable poly(L-lactic acid) (PLLA)/graphene oxide (GO) nanocomposites at different GO loadings from the amorphous state were investigated in detail in this work. During the nonisothermal cold crystallization, the crystallization peak temperature of PLLA shifts to low temperature range in the nanocomposites with increasing the GO loading relative to neat PLLA despite heating rate; moreover, the overall nonisothermal cold crystallization has been accelerated with increasing heating rate for both neat PLLA and its nanocomposites. In addition, the variations of crystallization enthalpy of PLLA during isothermal and nonisothermal cold crystallization processes were also discussed. Relative to neat PLLA, the overall isothermal cold crystallization rate of PLLA is increased with increasing the GO loading in the nanocomposites despite crystallization temperature. The crystallization rate becomes faster with increasing crystallization temperature, while the crystallization mechanism and crystal structure remain unchanged for both neat PLLA and its nanocomposites. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:229 / 236
页数:8
相关论文
共 35 条
[1]   Honeycomb Carbon: A Review of Graphene [J].
Allen, Matthew J. ;
Tung, Vincent C. ;
Kaner, Richard B. .
CHEMICAL REVIEWS, 2010, 110 (01) :132-145
[2]   Kinetics study of cold-crystallization of poly(ethylene terephthalate) nanocomposites with multi-walled carbon nanotubes [J].
Antoniadis, G. ;
Paraskevopoulos, K. M. ;
Bikiaris, D. ;
Chrissafis, K. .
THERMOCHIMICA ACTA, 2009, 493 (1-2) :68-75
[3]   Granulation, Phase Change, and Microstructure - Kinetics of Phase Change. III [J].
Avrami, M .
JOURNAL OF CHEMICAL PHYSICS, 1941, 9 (02) :177-184
[4]  
Avrami M., 1940, J. Chem. Phys, V8, P212, DOI [10.1063/1.1750631, DOI 10.1063/1.1750631]
[5]   The rise of graphene [J].
Geim, A. K. ;
Novoselov, K. S. .
NATURE MATERIALS, 2007, 6 (03) :183-191
[6]   Study of biodegradable polyactide/poly(butylene adipate-co-terephthalate) blends [J].
Jiang, L ;
Wolcott, MP ;
Zhang, JW .
BIOMACROMOLECULES, 2006, 7 (01) :199-207
[7]   Graphene/Polymer Nanocomposites [J].
Kim, Hyunwoo ;
Abdala, Ahmed A. ;
Macosko, Christopher W. .
MACROMOLECULES, 2010, 43 (16) :6515-6530
[8]   Graphene/Polyurethane Nanocomposites for Improved Gas Barrier and Electrical Conductivity [J].
Kim, Hyunwoo ;
Miura, Yutaka ;
Macosko, Christopher W. .
CHEMISTRY OF MATERIALS, 2010, 22 (11) :3441-3450
[9]   Polylactide/Exfoliated Graphite Nanocomposites with Enhanced Thermal Stability, Mechanical Modulus, and Electrical Conductivity [J].
Kim, Il-Hwan ;
Jeong, Young Gyu .
JOURNAL OF POLYMER SCIENCE PART B-POLYMER PHYSICS, 2010, 48 (08) :850-858
[10]   VARIATION OF PEAK TEMPERATURE WITH HEATING RATE IN DIFFERENTIAL THERMAL ANALYSIS [J].
KISSINGER, HE .
JOURNAL OF RESEARCH OF THE NATIONAL BUREAU OF STANDARDS, 1956, 57 (04) :217-221